HCID 131724410, compound → HCID 68453024, compound

HRID 2085736Notes

Reaction equation

HRID 2085736 reaction equation
[Si:1]([O:8][C:9]1[CH:10]=[CH:11][C:12](/[CH:19]=[CH:20]/[C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22])=[C:13]2[C:18]=1[N:17]=[CH:16][CH:15]=[CH:14]2)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2]>C1(C)C=CC=CC=1>[Si:1]([O:8][C:9]1[CH:10]=[CH:11][C:12]([CH2:19][CH2:20][C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22])=[C:13]2[C:18]=1[N:17]=[CH:16][CH:15]=[CH:14]2)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2]

Participants

3

Conditions

Temperature
60 °C

Procedure

A mixture of Example 201C (4.03 g, 10.5 mmol) and Rh(PPh3)3Cl (972 mg, 1.05 mmol) in toluene (40 mL) was degassed and flushed with hydrogen three times. The solution was heated to 60° C. under a hydrogen atmosphere for 16 hours and concentrated. The concentrate was purified by flash column chromatography on silica gel with 5-10% ethyl acetate/hexanes to provide the desired product.

Workup

  1. customflushed with hydrogen three times
  2. concentrationconcentrated
  3. customThe concentrate was purified by flash column chromatography on silica gel with 5-10% ethyl acetate/hexanes

Sources & evidence

ORD record
ord-9898acca33f84c1196da72f13b8a1ee5
Source dataset
uspto-grants-2004_04
Patent number
US06720338B2

Reaction notes

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